Canonical Allele Identifier: CA1335313980

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534034T= , CM000664.2:g.232534034T=	GRCh38
NC_000002.11:g.233398744T= , CM000664.1:g.233398744T=	GRCh37
NC_000002.10:g.233106988T=	NCBI36
NG_008028.1:g.12823T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1151T= MANE Select	ENSP00000258385.3:p.Ile384=
ENST00000258385.7:c.1151T=	ENSP00000258385.3:p.Ile384=
ENST00000441621.6:c.*333T=	ENSP00000408819.2:n.*333T=
ENST00000446616.1:c.*792T=	ENSP00000410801.1:n.*792T=
ENST00000543200.5:c.1106T=	ENSP00000438380.1:p.Ile369=
NM_000751.2:c.1151T=	NP_000742.1:p.Ile384=
NM_001256657.1:c.1106T=	NP_001243586.1:p.Ile369=
NM_001311195.1:c.569T=	NP_001298124.1:p.Ile190=
NM_001311196.1:c.848T=	NP_001298125.1:p.Ile283=
NR_046333.1:c.-4294966400T=
NR_046334.1:c.-4294966121T=
XM_011510524.1:c.770T=	XP_011508826.1:p.Ile257=
XM_011510524.2:c.770T=	XP_011508826.1:p.Ile257=
NM_000751.3:c.1151T= MANE Select	NP_000742.1:p.Ile384=
NM_001311195.2:c.569T=	NP_001298124.1:p.Ile190=
NM_001311196.2:c.848T=	NP_001298125.1:p.Ile283=
NM_001256657.2:c.1106T=	NP_001243586.1:p.Ile369=